Allele Registry

Canonical Allele Identifier: PA2825334745

Gene: NBN HGNC NCBI

ClinVar RCV:

RCV000131642

RCV000477065

RCV000485286

ClinVar Variation:

142497

HGVS (amino-acid)	Matching Registered Transcripts
NP_001019859.1:p.Met235Val	CA168521 NM_001024688.3:c.703A>G